Canonical Allele Identifier: CA824992670

Gene: AARS2 POLR1C

Linked Data

• dbSNP Id: rs1273670512
• gnomAD v3: 6-44310919-C-T
• gnomAD v4: 6-44310919-C-T
• MyVariant Identifiers: chr6:g.44278656C>T (hg19) ; chr6:g.44310919C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44310919C>T , CM000668.2:g.44310919C>T	GRCh38
NC_000006.11:g.44278656C>T , CM000668.1:g.44278656C>T	GRCh37
NC_000006.10:g.44386634C>T	NCBI36
NG_031952.1:g.7408G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000244571.5:c.749+75G>A (AARS2) MANE Select	ENSP00000244571.4:n.749+75G>A
ENST00000244571.4:c.749+75G>A (AARS2)	ENSP00000244571.4:n.749+75G>A
ENST00000505802.1:c.855+3277C>T
NM_020745.3:c.749+75G>A (AARS2)	NP_065796.1:n.749+75G>A
XM_005249245.2:c.749+75G>A (AARS2)	XP_005249302.1:n.749+75G>A
XM_011514764.1:c.749+75G>A (AARS2)	XP_011513066.1:n.749+75G>A
XR_241907.2:n.784+75G>A (AARS2)
XM_005249245.3:c.749+75G>A (AARS2)	XP_005249302.1:n.749+75G>A
XM_011514764.2:c.749+75G>A (AARS2)	XP_011513066.1:n.749+75G>A
XM_017011112.1:c.-270+75G>A (AARS2)	XP_016866601.1:n.-270+75G>A
NM_020745.4:c.749+75G>A (AARS2) MANE Select	NP_065796.2:n.749+75G>A
NM_001318876.2:c.946-130971C>T (POLR1C)	NP_001305805.1:n.946-130971C>T